FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DELMED IV CONTAINER

K Number: K830450 · Decision Mar 1, 1983
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
27
Review Days
14

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Basic Information

Device Name
DELMED IV CONTAINER
K Number
K830450
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Delmed, Inc.
Date Received
February 15, 1983
Decision Date
March 1, 1983
Product Code
KPE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPE Container, I.V.

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Other Clearances by Delmed, Inc.

K Number Device Name
K895142 ENTERAL PUMP SET WITH ENTERAL SPIKE
K895650 ENTERAL PUMP SET W/ENTERA-FLO SPIKE
K895329 600ML AND 1200ML ENTERAL BAG ADM. SET FOR ENTERA
K894506 ENTERA-FLO ENTERAL FEEDING PUMP
K901478 DELMED 80/2 DIALYSIS SYSTEM W/LAST BAG OPTION
K901477 DELMED 80/2 DIALYSIS SYSTEM W/ULTRAFILTRATION
K900106 CLOSED DISCONNECT SYSTEM
K895246 FRENTA(R) DUO-SET
K895330 600ML AND 1200ML ENTERAL BAG ADM. SET FOR FRENTA
K895919 ENTERAL BAG ADMINI. SETS FOR USE W/FLEXIFLO-III
Search all 27 clearances from Delmed, Inc. →